ライフサイエンスコーパス: pia

1 ssels, and in the dura mater, arachnoid, and pia mater of the meningeal sheath surrounding the optic

2 haracterized: dura-arachnoid enhancement and pia-subarachnoid space enhancement.

3 rane located between the neuroepithelium and pia-meninges.

4 l blood vessels and later within neurons and pia arachnoid (> or =3 hours), particularly within pirif

5 moniae iron uptake ABC transporters, piu and pia, resulted in a strain with impaired growth in two ty

6 treptonigrin of the individual pit, piu, and pia mutant strains and comparison of the growth in iron-

7 e astrocytes interact with blood vessels and pia, we suggest that such contact represents an early st

8 Gap junction coupling between pia-arachnoid cells and astrocytes was shown by dye tran

9 of overmigrated neurons into the developing pia-arachnoid, scattering its mesenchymal cells througho

10 t in basal laminae of the retina, epidermis, pia, cardiac and striated muscle, kidney, blood vessels,

11 recorded cell was estimated by distance from pia to the layer VI/white matter boundary, and verified

12 in layer VI when vertical cuts extended from pia mater through layers IV or V, but were no longer syn

13 cPLA2 mRNA was detected in pia mater, both at the brain surface and inner core of t

14 cells, and in the brain, it was expressed in pia matter and in neuronal tissues.

15 n subjects revealed IFITM mRNA expression in pia mater and blood vessels.

16 Calcium waves in pia-arachnoid cells could invade contiguous astrocytes,

17 es appear as the meninges differentiate into pia, arachnoid, and dura.

18 NMO-IgG outlines CNS microvessels, pia, subpia, and Virchow-Robin space.

19 oreceptor outer segments and the optic nerve pia and dura.

20 ing density was high in the olfactory nerve, pia mater, and aspects of the ventricular ependyma and w

21 rmation and further suggest a unique role of pia in cerebellar cortex histogenesis.

22 urogenesis and translocate to the overlaying pia, forming the indusium griseum.

23 nd emigrated neurons disrupted the overlying pia mater.

24 echanical stimulation of adult human and rat pia-arachnoid cell cultures (loaded with calcium indicat

25 pes were observed in layer I: Cajal Retzius, pia surface, vertical axon, and horizontal axon cells.

26 ingle and double mutant strains suggest that pia is the dominant iron transporter during in vitro and

27 The pia-arachnoid waves were blocked by either octanol or ap

28 landmarks, i.e., the barrels in Layer 4, the pia and white matter surfaces and the blood vessel patte

29 Because the pia mater and Purkinje cells sandwich the cerebellar EGL

30 that lie as far as 600 micrometers below the pia mater of primary somatosensory cortex in rat; this d

31 2(-/-) cell lines were implanted between the pia and arachnoid meninges as well as in the sciatic ner

32 n mast cells (or their precursors) enter the pia and access the thalamus by traveling along the ablum

33 then along blood vessels extending from the pia into the telencephalon on posthatch day 4-5, and in

34 he number of cells and microvessels from the pia to the white matter, show a significant correlation

35 shared by neuron ensembles spanning from the pia to the white matter.

36 nctionally similar neurons spanning from the pia to the white matter.

37 intense mGluR1 alpha immunoreactivity in the pia mater and blood vessels in the subarachnoid space an

38 t, in newborn mice, Ink4c is detected in the pia mater and in an adjacent layer of rapidly dividing c

39 new synthesis of elastin was present in the pia mater but not in astrocytes in the glial scar.

40 on, and creates small discontinuities in the pia mater overlying the tectum.

41 Staining was also observed in the pia matter, on a subpopulation of ependymal cells lining

42 Mast cells first appear in the pia on embryonic day (E)13-14 in ovo, then along blood v

43 The population in the pia reaches a maximum at postnatal (PN) day 11, and decl

44 disturbances that coincide with holes in the pia, and the caudomedial tectum exhibits prominent folds

45 uptake mechanisms, GABA transporters in the pia-arachnoid may help to regulate the amount of GABA av

46 The fraction of LC inserting into the pia (2.2%-29.6%) had a significant decrease with age (P

47 ecrease in the area of LC insertion into the pia (P = 0.55).

48 The LC inserted into the pia in all eyes.

49 ar implications of the LC insertion into the pia mater are not well understood and should be investig

50 The LC insertion into the pia mater is common in middle-aged and older eyes, and d

51 he peripapillary scleral flange and into the pia, and computed the total area of insertion and fracti

52 ertion and fraction of LC inserting into the pia.

53 that abnormalities in a region involving the pia mater and subpial cord occur early in the course of

54 ast cells occur in two locations, namely the pia and the brain parenchyma.

55 lted in widespread infection of cells of the pia and arachnoid mater of the leptomeninges over large

56 adhesion is critical for maintenance of the pia and proper cerebellar morphogenesis.

57 orresponding to the expected location of the pia mater and subpial region-and in spinal cord white an

58 ions requires a concomitant expansion of the pia mater.

59 gration defects leading to disruption of the pia-arachnoid, ectopia of fibroblasts in the cortex, and

60 ral fibers issued collateral branches to the pia at the frontal part of the brain.

61 , extend processes from the ventricle to the pia in regular parallel arrangements.

62 ortical parenchyma may be transmitted to the pia-arachnoid and might then serve in the induction of n

63 and 3 was almost entirely restricted to the pia-arachnoid, whereas mGATs 1 and 4 were present only i

64 spinal cord, from the ependymal layer to the pia-glial limitans, and from oligodendrocytes surroundin

65 lls in the more internal connective tissues (pia-arachnoid and endoneurium-perineurium) was also foun

66 ry itself does not bias activity flow toward pia.